Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D E Bulman

Showing results (11-20 of 52) with videos related to

Pageof 6
Sort By:
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 11, 2000
The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivationA F Struyk, K A Scoggan, D E Bulman, et al.
Advances in Experimental Medicine and Biology|January 1, 1990
Genetic and biochemical determinations in the pre-transplant workup and in the post-transplant assessment periodR G Worton, D E Bulman, E E Zubrzycka-Gaarn, et al.
Neurology|July 23, 2003
Mutations in the epsilon-sarcoglycan gene found to be uncommon in seven myoclonus-dystonia familiesF Han, A E Lang, L Racacho, et al.
Journal of Medical Genetics|May 24, 2001
Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2K A Scoggan, T Chandra, R Nelson, et al.
Archives of Neurology|June 1, 1991
The influence of gender on the susceptibility to multiple sclerosis in sibshipsA D Sadovnick, D E Bulman, L Hashimoto, et al.
Epilepsia|February 26, 2000
Evidence favoring genetic heterogeneity for febrile convulsionsL J Racacho, R S McLachlan, G C Ebers, et al.
Neurology|September 1, 1992
Premature chain termination mutation causing Duchenne muscular dystrophyP R Clemens, P A Ward, C T Caskey, et al.
Annals of Neurology|October 1, 1986
Absence of antibody to HTLV I and III in sera of Canadian patients with multiple sclerosis and chronic myelopathyG P Rice, H A Armstrong, D E Bulman, et al.
Human Molecular Genetics|February 1, 1995
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19pB von Brederlow, A F Hahn, W J Koopman, et al.
American Journal of Human Genetics|June 1, 1989
Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy geneX Y Hu, A H Burghes, D E Bulman, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 11, 2000
The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivationA F Struyk, K A Scoggan, D E Bulman, et al.
Advances in Experimental Medicine and Biology|January 1, 1990
Genetic and biochemical determinations in the pre-transplant workup and in the post-transplant assessment periodR G Worton, D E Bulman, E E Zubrzycka-Gaarn, et al.
Neurology|July 23, 2003
Mutations in the epsilon-sarcoglycan gene found to be uncommon in seven myoclonus-dystonia familiesF Han, A E Lang, L Racacho, et al.
Journal of Medical Genetics|May 24, 2001
Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2K A Scoggan, T Chandra, R Nelson, et al.
Archives of Neurology|June 1, 1991
The influence of gender on the susceptibility to multiple sclerosis in sibshipsA D Sadovnick, D E Bulman, L Hashimoto, et al.
Epilepsia|February 26, 2000
Evidence favoring genetic heterogeneity for febrile convulsionsL J Racacho, R S McLachlan, G C Ebers, et al.
Neurology|September 1, 1992
Premature chain termination mutation causing Duchenne muscular dystrophyP R Clemens, P A Ward, C T Caskey, et al.
Annals of Neurology|October 1, 1986
Absence of antibody to HTLV I and III in sera of Canadian patients with multiple sclerosis and chronic myelopathyG P Rice, H A Armstrong, D E Bulman, et al.
Human Molecular Genetics|February 1, 1995
Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19pB von Brederlow, A F Hahn, W J Koopman, et al.
American Journal of Human Genetics|June 1, 1989
Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy geneX Y Hu, A H Burghes, D E Bulman, et al.
Pageof 6